-
2
-
-
0141703263
-
Independent beta-arrestin 2 and G protein-mediated pathways for angiotensin II activation of extracellular signal-regulated kinases 1 and 2
-
Wei, H.; Ahn, S.; Shenoy, S. K.; Karnik, S. S.; Hunyady, L.; Luttrell, L. M.; Lefkowitz, R. J. Independent beta-arrestin 2 and G protein-mediated pathways for angiotensin II activation of extracellular signal-regulated kinases 1 and 2 Proc. Natl. Acad. Sci. U.S.A. 2003, 100, 10782-10787
-
(2003)
Proc. Natl. Acad. Sci. U.S.A.
, vol.100
, pp. 10782-10787
-
-
Wei, H.1
Ahn, S.2
Shenoy, S.K.3
Karnik, S.S.4
Hunyady, L.5
Luttrell, L.M.6
Lefkowitz, R.J.7
-
3
-
-
17644402459
-
Transduction of receptor signals by beta-arrestins
-
Lefkowitz, R. J.; Shenoy, S. K. Transduction of receptor signals by beta-arrestins Science 2005, 308, 512-517
-
(2005)
Science
, vol.308
, pp. 512-517
-
-
Lefkowitz, R.J.1
Shenoy, S.K.2
-
5
-
-
84877631485
-
Structural features for functional selectivity at serotonin receptors
-
Wacker, D.; Wang, C.; Katritch, V.; Han, G. W.; Huang, X. P.; Vardy, E.; McCorvy, J. D.; Jiang, Y.; Chu, M.; Siu, F. Y.; Liu, W.; Xu, H. E.; Cherezov, V.; Roth, B. L.; Stevens, R. C. Structural features for functional selectivity at serotonin receptors Science 2013, 340, 615-619
-
(2013)
Science
, vol.340
, pp. 615-619
-
-
Wacker, D.1
Wang, C.2
Katritch, V.3
Han, G.W.4
Huang, X.P.5
Vardy, E.6
McCorvy, J.D.7
Jiang, Y.8
Chu, M.9
Siu, F.Y.10
Liu, W.11
Xu, H.E.12
Cherezov, V.13
Roth, B.L.14
Stevens, R.C.15
-
6
-
-
81055145330
-
Discovery of beta-arrestin-biased dopamine D2 ligands for probing signal transduction pathways essential for antipsychotic efficacy
-
Allen, J. A.; Yost, J. M.; Setola, V.; Chen, X.; Sassano, M. F.; Chen, M.; Peterson, S.; Yadav, P. N.; Huang, X. P.; Feng, B.; Jensen, N. H.; Che, X.; Bai, X.; Frye, S. V.; Wetsel, W. C.; Caron, M. G.; Javitch, J. A.; Roth, B. L.; Jin, J. Discovery of beta-arrestin-biased dopamine D2 ligands for probing signal transduction pathways essential for antipsychotic efficacy Proc. Natl. Acad. Sci. U.S.A. 2011, 108, 18488-18493
-
(2011)
Proc. Natl. Acad. Sci. U.S.A.
, vol.108
, pp. 18488-18493
-
-
Allen, J.A.1
Yost, J.M.2
Setola, V.3
Chen, X.4
Sassano, M.F.5
Chen, M.6
Peterson, S.7
Yadav, P.N.8
Huang, X.P.9
Feng, B.10
Jensen, N.H.11
Che, X.12
Bai, X.13
Frye, S.V.14
Wetsel, W.C.15
Caron, M.G.16
Javitch, J.A.17
Roth, B.L.18
Jin, J.19
-
7
-
-
84866934645
-
Structure-functional selectivity relationship studies of beta-arrestin-biased dopamine D(2) receptor agonists
-
Chen, X.; Sassano, M. F.; Zheng, L.; Setola, V.; Chen, M.; Bai, X.; Frye, S. V.; Wetsel, W. C.; Roth, B. L.; Jin, J. Structure-functional selectivity relationship studies of beta-arrestin-biased dopamine D(2) receptor agonists J. Med. Chem. 2012, 55, 7141-7153
-
(2012)
J. Med. Chem.
, vol.55
, pp. 7141-7153
-
-
Chen, X.1
Sassano, M.F.2
Zheng, L.3
Setola, V.4
Chen, M.5
Bai, X.6
Frye, S.V.7
Wetsel, W.C.8
Roth, B.L.9
Jin, J.10
-
8
-
-
51649084026
-
Antagonism of dopamine D2 receptor/beta-arrestin 2 interaction is a common property of clinically effective antipsychotics
-
Masri, B.; Salahpour, A.; Didriksen, M.; Ghisi, V.; Beaulieu, J. M.; Gainetdinov, R. R.; Caron, M. G. Antagonism of dopamine D2 receptor/beta- arrestin 2 interaction is a common property of clinically effective antipsychotics Proc. Natl. Acad. Sci. U.S.A. 2008, 105, 13656-13661
-
(2008)
Proc. Natl. Acad. Sci. U.S.A.
, vol.105
, pp. 13656-13661
-
-
Masri, B.1
Salahpour, A.2
Didriksen, M.3
Ghisi, V.4
Beaulieu, J.M.5
Gainetdinov, R.R.6
Caron, M.G.7
-
9
-
-
0035101404
-
Antipsychotic drugs: Importance of dopamine receptors for mechanisms of therapeutic actions and side effects
-
Strange, P. G. Antipsychotic drugs: importance of dopamine receptors for mechanisms of therapeutic actions and side effects Pharmacol. Rev. 2001, 53, 119-133
-
(2001)
Pharmacol. Rev.
, vol.53
, pp. 119-133
-
-
Strange, P.G.1
-
10
-
-
21544439847
-
Dopamine D3 receptor antagonists as therapeutic agents
-
Joyce, J. N.; Millan, M. J. Dopamine D3 receptor antagonists as therapeutic agents Drug Discovery Today 2005, 10, 917-925
-
(2005)
Drug Discovery Today
, vol.10
, pp. 917-925
-
-
Joyce, J.N.1
Millan, M.J.2
-
11
-
-
33846905526
-
Recent progress in development of dopamine receptor subtype-selective agents: Potential therapeutics for neurological and psychiatric disorders
-
Zhang, A.; Neumeyer, J. L.; Baldessarini, R. J. Recent progress in development of dopamine receptor subtype-selective agents: potential therapeutics for neurological and psychiatric disorders Chem. Rev. 2007, 107, 274-302
-
(2007)
Chem. Rev.
, vol.107
, pp. 274-302
-
-
Zhang, A.1
Neumeyer, J.L.2
Baldessarini, R.J.3
-
12
-
-
77949300041
-
Current perspectives on selective dopamine D(3) receptor antagonists as pharmacotherapeutics for addictions and related disorders
-
Heidbreder, C. A.; Newman, A. H. Current perspectives on selective dopamine D(3) receptor antagonists as pharmacotherapeutics for addictions and related disorders Ann. N.Y. Acad. Sci. 2010, 1187, 4-34
-
(2010)
Ann. N.Y. Acad. Sci.
, vol.1187
, pp. 4-34
-
-
Heidbreder, C.A.1
Newman, A.H.2
-
13
-
-
79952032110
-
The physiology, signaling, and pharmacology of dopamine receptors
-
Beaulieu, J. M.; Gainetdinov, R. R. The physiology, signaling, and pharmacology of dopamine receptors Pharmacol. Rev. 2011, 63, 182-217
-
(2011)
Pharmacol. Rev.
, vol.63
, pp. 182-217
-
-
Beaulieu, J.M.1
Gainetdinov, R.R.2
-
14
-
-
41149164277
-
G protein coupling and ligand selectivity of the D2L and D3 dopamine receptors
-
Lane, J. R.; Powney, B.; Wise, A.; Rees, S.; Milligan, G. G protein coupling and ligand selectivity of the D2L and D3 dopamine receptors J. Pharmacol. Exp. Ther. 2008, 325, 319-330
-
(2008)
J. Pharmacol. Exp. Ther.
, vol.325
, pp. 319-330
-
-
Lane, J.R.1
Powney, B.2
Wise, A.3
Rees, S.4
Milligan, G.5
-
15
-
-
0037350667
-
Functional coupling of the human dopamine D2 receptor with G alpha i1, G alpha i2, G alpha i3 and G alpha o G proteins: Evidence for agonist regulation of G protein selectivity
-
Gazi, L.; Nickolls, S. A.; Strange, P. G. Functional coupling of the human dopamine D2 receptor with G alpha i1, G alpha i2, G alpha i3 and G alpha o G proteins: evidence for agonist regulation of G protein selectivity Br. J. Pharmacol. 2003, 138, 775-786
-
(2003)
Br. J. Pharmacol.
, vol.138
, pp. 775-786
-
-
Gazi, L.1
Nickolls, S.A.2
Strange, P.G.3
-
16
-
-
0035853047
-
Most central nervous system D2 dopamine receptors are coupled to their effectors by Go
-
Jiang, M.; Spicher, K.; Boulay, G.; Wang, Y.; Birnbaumer, L. Most central nervous system D2 dopamine receptors are coupled to their effectors by Go Proc. Natl. Acad. Sci. U.S.A. 2001, 98, 3577-3582
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 3577-3582
-
-
Jiang, M.1
Spicher, K.2
Boulay, G.3
Wang, Y.4
Birnbaumer, L.5
-
17
-
-
60149091355
-
Molecular mechanisms of go signaling
-
Jiang, M.; Bajpayee, N. S. Molecular mechanisms of go signaling Neurosignals 2009, 17, 23-41
-
(2009)
Neurosignals
, vol.17
, pp. 23-41
-
-
Jiang, M.1
Bajpayee, N.S.2
-
18
-
-
0028359453
-
G protein specificity in receptor-effector coupling. Analysis of the roles of G0 and Gi2 in GH4C1 pituitary cells
-
Liu, Y. F.; Jakobs, K. H.; Rasenick, M. M.; Albert, P. R. G protein specificity in receptor-effector coupling. Analysis of the roles of G0 and Gi2 in GH4C1 pituitary cells J. Biol. Chem. 1994, 269, 13880-13886
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 13880-13886
-
-
Liu, Y.F.1
Jakobs, K.H.2
Rasenick, M.M.3
Albert, P.R.4
-
19
-
-
0033515116
-
Distinct roles for Galphai2, Galphai3, and Gbeta gamma in modulation offorskolin- or Gs-mediated cAMP accumulation and calcium mobilization by dopamine D2S receptors
-
Ghahremani, M. H.; Cheng, P.; Lembo, P. M.; Albert, P. R. Distinct roles for Galphai2, Galphai3, and Gbeta gamma in modulation offorskolin- or Gs-mediated cAMP accumulation and calcium mobilization by dopamine D2S receptors J. Biol. Chem. 1999, 274, 9238-9245
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 9238-9245
-
-
Ghahremani, M.H.1
Cheng, P.2
Lembo, P.M.3
Albert, P.R.4
-
20
-
-
0033622132
-
Distinct roles for Galpha(i)2 and Gbetagamma in signaling to DNA synthesis and Galpha(i)3 in cellular transformation by dopamine D2S receptor activation in BALB/c 3T3 cells
-
Ghahremani, M. H.; Forget, C.; Albert, P. R. Distinct roles for Galpha(i)2 and Gbetagamma in signaling to DNA synthesis and Galpha(i)3 in cellular transformation by dopamine D2S receptor activation in BALB/c 3T3 cells Mol. Cell. Biol. 2000, 20, 1497-1506
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 1497-1506
-
-
Ghahremani, M.H.1
Forget, C.2
Albert, P.R.3
-
21
-
-
55549086457
-
Roles of G protein and beta-arrestin in dopamine D2 receptor-mediated ERK activation
-
Quan, W.; Kim, J. H.; Albert, P. R.; Choi, H.; Kim, K. M. Roles of G protein and beta-arrestin in dopamine D2 receptor-mediated ERK activation Biochem. Biophys. Res. Commun. 2008, 377, 705-709
-
(2008)
Biochem. Biophys. Res. Commun.
, vol.377
, pp. 705-709
-
-
Quan, W.1
Kim, J.H.2
Albert, P.R.3
Choi, H.4
Kim, K.M.5
-
22
-
-
0035800852
-
Agonist regulation of D(2) dopamine receptor/G protein interaction. Evidence for agonist selection of G protein subtype
-
Cordeaux, Y.; Nickolls, S. A.; Flood, L. A.; Graber, S. G.; Strange, P. G. Agonist regulation of D(2) dopamine receptor/G protein interaction. Evidence for agonist selection of G protein subtype J. Biol. Chem. 2001, 276, 28667-28675
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 28667-28675
-
-
Cordeaux, Y.1
Nickolls, S.A.2
Flood, L.A.3
Graber, S.G.4
Strange, P.G.5
-
23
-
-
79952454207
-
Recent advances in the search for D3- and D4-selective drugs: Probes, models and candidates
-
Lober, S.; Hubner, H.; Tschammer, N.; Gmeiner, P. Recent advances in the search for D3- and D4-selective drugs: probes, models and candidates Trends Pharmacol. Sci. 2011, 32, 148-157
-
(2011)
Trends Pharmacol. Sci.
, vol.32
, pp. 148-157
-
-
Lober, S.1
Hubner, H.2
Tschammer, N.3
Gmeiner, P.4
-
24
-
-
79951972094
-
Histidine 6.55 is a major determinant of ligand-biased signaling in dopamine D2L receptor
-
Tschammer, N.; Bollinger, S.; Kenakin, T.; Gmeiner, P. Histidine 6.55 is a major determinant of ligand-biased signaling in dopamine D2L receptor Mol. Pharmacol. 2011, 79, 575-585
-
(2011)
Mol. Pharmacol.
, vol.79
, pp. 575-585
-
-
Tschammer, N.1
Bollinger, S.2
Kenakin, T.3
Gmeiner, P.4
-
25
-
-
0038248584
-
Conjugated enynes as nonaromatic catechol bioisosteres: Synthesis, binding experiments, and computational studies of novel dopamine receptor agonists recognizing preferentially the D-3 subtype
-
Hubner, H.; Haubmann, C.; Utz, W.; Gmeiner, P. Conjugated enynes as nonaromatic catechol bioisosteres: synthesis, binding experiments, and computational studies of novel dopamine receptor agonists recognizing preferentially the D-3 subtype J. Med. Chem. 2000, 43, 756-762
-
(2000)
J. Med. Chem.
, vol.43
, pp. 756-762
-
-
Hubner, H.1
Haubmann, C.2
Utz, W.3
Gmeiner, P.4
-
26
-
-
0346671325
-
Analogues of FAUC 73 revealing new insights into the structural requirements of nonaromatic dopamine D3 receptor agonists
-
Lenz, C.; Boeckler, F.; Hubner, H.; Gmeiner, P. Analogues of FAUC 73 revealing new insights into the structural requirements of nonaromatic dopamine D3 receptor agonists Bioorg. Med. Chem. 2004, 12, 113-117
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 113-117
-
-
Lenz, C.1
Boeckler, F.2
Hubner, H.3
Gmeiner, P.4
-
27
-
-
9644276854
-
Fancy bioisosteres: Synthesis and dopaminergic properties of the endiyne FAUC 88 as a novel non-aromatic D3 agonist
-
Lenz, C.; Haubmann, C.; Hubner, H.; Boeckler, F.; Gmeiner, P. Fancy bioisosteres: synthesis and dopaminergic properties of the endiyne FAUC 88 as a novel non-aromatic D3 agonist Bioorg. Med. Chem. 2005, 13, 185-191
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 185-191
-
-
Lenz, C.1
Haubmann, C.2
Hubner, H.3
Boeckler, F.4
Gmeiner, P.5
-
28
-
-
20444468075
-
Fancy bioisosteres: Synthesis, SAR, and pharmacological investigations of novel nonaromatic dopamine D3 receptor ligands
-
Lenz, C.; Boeckler, F.; Hubner, H.; Gmeiner, P. Fancy bioisosteres: synthesis, SAR, and pharmacological investigations of novel nonaromatic dopamine D3 receptor ligands Bioorg. Med. Chem. 2005, 13, 4434-4442
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 4434-4442
-
-
Lenz, C.1
Boeckler, F.2
Hubner, H.3
Gmeiner, P.4
-
29
-
-
56249118049
-
Novel D3 selective dopaminergics incorporating enyne units as nonaromatic catechol bioisosteres: Synthesis, bioactivity, and mutagenesis studies
-
Dorfler, M.; Tschammer, N.; Hamperl, K.; Hubner, H.; Gmeiner, P. Novel D3 selective dopaminergics incorporating enyne units as nonaromatic catechol bioisosteres: synthesis, bioactivity, and mutagenesis studies J. Med. Chem. 2008, 51, 6829-6838
-
(2008)
J. Med. Chem.
, vol.51
, pp. 6829-6838
-
-
Dorfler, M.1
Tschammer, N.2
Hamperl, K.3
Hubner, H.4
Gmeiner, P.5
-
30
-
-
68949147023
-
Facile conversion of primary and secondary alcohols to alkyl iodides
-
Lange, G. L.; Gottardo, C. Facile conversion of primary and secondary alcohols to alkyl iodides Synth. Commun. 1990, 20, 1473-1479
-
(1990)
Synth. Commun.
, vol.20
, pp. 1473-1479
-
-
Lange, G.L.1
Gottardo, C.2
-
31
-
-
35348850316
-
Investigating direct access to 2-oxospiro[4.5]decanones via 6 pi-electrocyclisation
-
Pouwer, R. H.; Schill, H.; Williams, C. M.; Bernhardt, P. V. Investigating direct access to 2-oxospiro[4.5]decanones via 6 pi-electrocyclisation Eur. J. Org. Chem. 2007, 4699-4705
-
(2007)
Eur. J. Org. Chem.
, pp. 4699-4705
-
-
Pouwer, R.H.1
Schill, H.2
Williams, C.M.3
Bernhardt, P.V.4
-
32
-
-
81555228201
-
Development of a bivalent dopamine D2 receptor agonist
-
Kuhhorn, J.; Gotz, A.; Hubner, H.; Thompson, D.; Whistler, J.; Gmeiner, P. Development of a bivalent dopamine D2 receptor agonist J. Med. Chem. 2011, 54, 7911-7919
-
(2011)
J. Med. Chem.
, vol.54
, pp. 7911-7919
-
-
Kuhhorn, J.1
Gotz, A.2
Hubner, H.3
Thompson, D.4
Whistler, J.5
Gmeiner, P.6
-
33
-
-
0013624593
-
Sulfur trioxide in the oxidation of alcohols by dimethyl sulfoxide
-
Parikh, J. R.; Doering, W. v. E. Sulfur trioxide in the oxidation of alcohols by dimethyl sulfoxide J. Am. Chem. Soc. 1967, 89, 5505-5507
-
(1967)
J. Am. Chem. Soc.
, vol.89
, pp. 5505-5507
-
-
Parikh, J.R.1
Doering, V.W.E.2
-
34
-
-
0030753786
-
In vitro identification of the P450 enzymes responsible for the metabolism of ropinirole
-
Bloomer, J. C.; Clarke, S. E.; Chenery, R. J. In vitro identification of the P450 enzymes responsible for the metabolism of ropinirole Drug Metab. Dispos. 1997, 25, 840-844
-
(1997)
Drug Metab. Dispos.
, vol.25
, pp. 840-844
-
-
Bloomer, J.C.1
Clarke, S.E.2
Chenery, R.J.3
-
35
-
-
0033025007
-
Disposition of ropinirole in animals and man
-
Ramji, J. V.; Keogh, J. P.; Blake, T. J.; Broom, C.; Chenery, R. J.; Citerone, D. R.; Lewis, V. A.; Taylor, A. C.; Yeulet, S. E. Disposition of ropinirole in animals and man Xenobiotica 1999, 29, 311-325
-
(1999)
Xenobiotica
, vol.29
, pp. 311-325
-
-
Ramji, J.V.1
Keogh, J.P.2
Blake, T.J.3
Broom, C.4
Chenery, R.J.5
Citerone, D.R.6
Lewis, V.A.7
Taylor, A.C.8
Yeulet, S.E.9
-
36
-
-
70349302129
-
Absorption, disposition, metabolic fate, and elimination of the dopamine agonist rotigotine in man: Administration by intravenous infusion or transdermal delivery
-
Cawello, W.; Braun, M.; Boekens, H. Absorption, disposition, metabolic fate, and elimination of the dopamine agonist rotigotine in man: administration by intravenous infusion or transdermal delivery Drug Metab. Dispos. 2009, 37, 2055-2060
-
(2009)
Drug Metab. Dispos.
, vol.37
, pp. 2055-2060
-
-
Cawello, W.1
Braun, M.2
Boekens, H.3
-
37
-
-
0028181472
-
Determination of the dopamine-D2 agonist N-0923 and Its major metabolites in perfused rat livers by HPLC UV atmospheric-pressure ionization mass-spectrometry
-
Swart, P. J.; Oelen, W. E. M.; Bruins, A. P.; Tepper, P. G.; Dezeeuw, R. A. Determination of the dopamine-D2 agonist N-0923 and Its major metabolites in perfused rat livers by HPLC UV atmospheric-pressure ionization mass-spectrometry J. Anal. Toxicol. 1994, 18, 71-77
-
(1994)
J. Anal. Toxicol.
, vol.18
, pp. 71-77
-
-
Swart, P.J.1
Oelen, W.E.M.2
Bruins, A.P.3
Tepper, P.G.4
Dezeeuw, R.A.5
-
38
-
-
0034464799
-
Pre-clinical studies of pramipexole: Clinical relevance
-
Hubble, J. P. Pre-clinical studies of pramipexole: clinical relevance Eur. J. Neurol. 2000, 7, 15-20
-
(2000)
Eur. J. Neurol.
, vol.7
, pp. 15-20
-
-
Hubble, J.P.1
-
39
-
-
0021854707
-
Metabolism and disposition of the dopaminergic agonist 5-hydroxy-6-methyl-2-di-normal-propylaminotetralin in the rat
-
Koble, D. L.; Koons, J. C.; Fischer, L. J. Metabolism and disposition of the dopaminergic agonist 5-hydroxy-6-methyl-2-di-normal-propylaminotetralin in the rat Drug Metab. Dispos. 1985, 13, 305-311
-
(1985)
Drug Metab. Dispos.
, vol.13
, pp. 305-311
-
-
Koble, D.L.1
Koons, J.C.2
Fischer, L.J.3
-
40
-
-
0025644730
-
Metabolism of antiparkinson agent dopazinol by rat-liver microsomes
-
Vyas, K. P.; Kari, P. H.; Ramjit, H. G.; Pitzenberger, S. M.; Hichens, M. Metabolism of antiparkinson agent dopazinol by rat-liver microsomes Drug Metab. Dispos. 1990, 18, 1025-1030
-
(1990)
Drug Metab. Dispos.
, vol.18
, pp. 1025-1030
-
-
Vyas, K.P.1
Kari, P.H.2
Ramjit, H.G.3
Pitzenberger, S.M.4
Hichens, M.5
-
41
-
-
0036827811
-
Differential actions of antiparkinson agents at multiple classes of monoaminergic receptor. I. A multivariate analysis of the binding profiles of 14 drugs at 21 native and cloned human receptor subtypes
-
Millan, M. J.; Maiofiss, L.; Cussac, D.; Audinot, V.; Boutin, J. A.; Newman-Tancredi, A. Differential actions of antiparkinson agents at multiple classes of monoaminergic receptor. I. A multivariate analysis of the binding profiles of 14 drugs at 21 native and cloned human receptor subtypes J. Pharmacol. Exp. Ther. 2002, 303, 791-804
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.303
, pp. 791-804
-
-
Millan, M.J.1
Maiofiss, L.2
Cussac, D.3
Audinot, V.4
Boutin, J.A.5
Newman-Tancredi, A.6
-
42
-
-
0028128734
-
The D2 dopamine receptor isoforms signal through distinct Gi alpha proteins to inhibit adenylyl cyclase. A study with site-directed mutant Gi alpha proteins
-
Senogles, S. E. The D2 dopamine receptor isoforms signal through distinct Gi alpha proteins to inhibit adenylyl cyclase. A study with site-directed mutant Gi alpha proteins J. Biol. Chem. 1994, 269, 23120-23127
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 23120-23127
-
-
Senogles, S.E.1
-
43
-
-
78449305788
-
Structure of the human dopamine D3 receptor in complex with a D2/D3 selective antagonist
-
Chien, E. Y.; Liu, W.; Zhao, Q.; Katritch, V.; Han, G. W.; Hanson, M. A.; Shi, L.; Newman, A. H.; Javitch, J. A.; Cherezov, V.; Stevens, R. C. Structure of the human dopamine D3 receptor in complex with a D2/D3 selective antagonist Science 2010, 330, 1091-1095
-
(2010)
Science
, vol.330
, pp. 1091-1095
-
-
Chien, E.Y.1
Liu, W.2
Zhao, Q.3
Katritch, V.4
Han, G.W.5
Hanson, M.A.6
Shi, L.7
Newman, A.H.8
Javitch, J.A.9
Cherezov, V.10
Stevens, R.C.11
-
44
-
-
78549272001
-
The minor binding pocket: A major player in 7TM receptor activation
-
Rosenkilde, M. M.; Benned-Jensen, T.; Frimurer, T. M.; Schwartz, T. W. The minor binding pocket: a major player in 7TM receptor activation Trends Pharmacol. Sci. 2010, 31, 567-574
-
(2010)
Trends Pharmacol. Sci.
, vol.31
, pp. 567-574
-
-
Rosenkilde, M.M.1
Benned-Jensen, T.2
Frimurer, T.M.3
Schwartz, T.W.4
-
45
-
-
84877607189
-
Structural basis for molecular recognition at serotonin receptors
-
Wang, C.; Jiang, Y.; Ma, J.; Wu, H.; Wacker, D.; Katritch, V.; Han, G. W.; Liu, W.; Huang, X. P.; Vardy, E.; McCorvy, J. D.; Gao, X.; Zhou, X. E.; Melcher, K.; Zhang, C.; Bai, F.; Yang, H.; Yang, L.; Jiang, H.; Roth, B. L.; Cherezov, V.; Stevens, R. C.; Xu, H. E. Structural basis for molecular recognition at serotonin receptors Science 2013, 340, 610-614
-
(2013)
Science
, vol.340
, pp. 610-614
-
-
Wang, C.1
Jiang, Y.2
Ma, J.3
Wu, H.4
Wacker, D.5
Katritch, V.6
Han, G.W.7
Liu, W.8
Huang, X.P.9
Vardy, E.10
McCorvy, J.D.11
Gao, X.12
Zhou, X.E.13
Melcher, K.14
Zhang, C.15
Bai, F.16
Yang, H.17
Yang, L.18
Jiang, H.19
Roth, B.L.20
Cherezov, V.21
Stevens, R.C.22
Xu, H.E.23
more..
-
46
-
-
0026763185
-
Synthetic and mechanistic studies on the antitumor antibiotics esperamicin-A1 and calicheamicin-gamma-1. Synthesis of 2-letobicyclo[7.3.1] enediyne and 13-ketocyclo[7.3.1] enediyne cores mediated by eta-2 dicobalt hexacarbonyl alkyne complexes. Cycloaromatization rate studies
-
Magnus, P.; Carter, P.; Elliott, J.; Lewis, R.; Harling, J.; Pitterna, T.; Bauta, W. E.; Fortt, S. Synthetic and mechanistic studies on the antitumor antibiotics esperamicin-A1 and calicheamicin-gamma-1. Synthesis of 2-letobicyclo[7.3.1] enediyne and 13-ketocyclo[7.3.1] enediyne cores mediated by eta-2 dicobalt hexacarbonyl alkyne complexes. Cycloaromatization rate studies J. Am. Chem. Soc. 1992, 114, 2544-2559
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 2544-2559
-
-
Magnus, P.1
Carter, P.2
Elliott, J.3
Lewis, R.4
Harling, J.5
Pitterna, T.6
Bauta, W.E.7
Fortt, S.8
-
47
-
-
84892671444
-
New synthesis of 1,4-dihydroxybicyclo[2.2.2]octane
-
Geivandov, R. K.; Kovshev, E. I. New synthesis of 1,4-dihydroxybicyclo[2. 2.2]octane Zh. Org. Khim. 1979, 15, 218-219
-
(1979)
Zh. Org. Khim.
, vol.15
, pp. 218-219
-
-
Geivandov, R.K.1
Kovshev, E.I.2
-
49
-
-
35148898301
-
Hybrid approach for the design of highly affine and selective dopamine D-3 receptor ligands using privileged scaffolds of biogenic amine GPCR ligands
-
Sasse, B. C.; Mach, U. R.; Leppaenen, J.; Calmels, T.; Stark, H. Hybrid approach for the design of highly affine and selective dopamine D-3 receptor ligands using privileged scaffolds of biogenic amine GPCR ligands Bioorg. Med. Chem. 2007, 15, 7258-7273
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 7258-7273
-
-
Sasse, B.C.1
Mach, U.R.2
Leppaenen, J.3
Calmels, T.4
Stark, H.5
-
50
-
-
84879558254
-
-
WO2009/056805A1
-
Stark, H.; Leppanen, J. M.; Sasse, B. C.; Saur, O.; Kottke, T.; Hill, M. P. Medicaments. WO2009/056805A1, 2009.
-
(2009)
Medicaments
-
-
Stark, H.1
Leppanen, J.M.2
Sasse, B.C.3
Saur, O.4
Kottke, T.5
Hill, M.P.6
-
51
-
-
79953775165
-
Highly potent 5-aminotetrahydropyrazolopyridines: Enantioselective dopamine D-3 receptor binding, functional selectivity, and analysis of receptor-ligand interactions
-
Tschammer, N.; Elsner, J.; Goetz, A.; Ehrlich, K.; Schuster, S.; Ruberg, M.; Kuhhorn, J.; Thompson, D.; Whistler, J.; Hubner, H.; Gmeiner, P. Highly potent 5-aminotetrahydropyrazolopyridines: enantioselective dopamine D-3 receptor binding, functional selectivity, and analysis of receptor-ligand interactions J. Med. Chem. 2011, 54, 2477-2491
-
(2011)
J. Med. Chem.
, vol.54
, pp. 2477-2491
-
-
Tschammer, N.1
Elsner, J.2
Goetz, A.3
Ehrlich, K.4
Schuster, S.5
Ruberg, M.6
Kuhhorn, J.7
Thompson, D.8
Whistler, J.9
Hubner, H.10
Gmeiner, P.11
-
52
-
-
0026695537
-
Structural subtypes of the dopamine D2 receptor are functionally distinct: Expression of the cloned D2A and D2B subtypes in a heterologous cell line
-
Hayes, G.; Biden, T. J.; Selbie, L. A.; Shine, J. Structural subtypes of the dopamine D2 receptor are functionally distinct: expression of the cloned D2A and D2B subtypes in a heterologous cell line Mol. Endocrinol. 1992, 6, 920-926
-
(1992)
Mol. Endocrinol.
, vol.6
, pp. 920-926
-
-
Hayes, G.1
Biden, T.J.2
Selbie, L.A.3
Shine, J.4
-
53
-
-
0025179967
-
Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neuroleptics
-
Sokoloff, P.; Giros, B.; Martres, M. P.; Bouthenet, M. L.; Schwartz, J. C. Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neuroleptics Nature 1990, 347, 146-151
-
(1990)
Nature
, vol.347
, pp. 146-151
-
-
Sokoloff, P.1
Giros, B.2
Martres, M.P.3
Bouthenet, M.L.4
Schwartz, J.C.5
-
54
-
-
0029120447
-
Modulation of intracellular cyclic AMP levels by different human dopamine D4 receptor variants
-
Asghari, V.; Sanyal, S.; Buchwaldt, S.; Paterson, A.; Jovanovic, V.; Van Tol, H. H. Modulation of intracellular cyclic AMP levels by different human dopamine D4 receptor variants J. Neurochem. 1995, 65, 1157-1165
-
(1995)
J. Neurochem.
, vol.65
, pp. 1157-1165
-
-
Asghari, V.1
Sanyal, S.2
Buchwaldt, S.3
Paterson, A.4
Jovanovic, V.5
Van Tol, H.H.6
-
55
-
-
0037057547
-
Interactive SAR studies: Rational discovery of super-potent and highly selective dopamine D3 receptor antagonists and partial agonists
-
Bettinetti, L.; Schlotter, K.; Hubner, H.; Gmeiner, P. Interactive SAR studies: rational discovery of super-potent and highly selective dopamine D3 receptor antagonists and partial agonists J. Med. Chem. 2002, 45, 4594-4597
-
(2002)
J. Med. Chem.
, vol.45
, pp. 4594-4597
-
-
Bettinetti, L.1
Schlotter, K.2
Hubner, H.3
Gmeiner, P.4
-
56
-
-
71849104860
-
Protein measurement with the folin phenol reagent
-
Lowry, O. H.; Rosebrough, N. J.; Farr, A. L.; Randall, R. J. Protein measurement with the folin phenol reagent J. Biol. Chem. 1951, 193, 265-275
-
(1951)
J. Biol. Chem.
, vol.193
, pp. 265-275
-
-
Lowry, O.H.1
Rosebrough, N.J.2
Farr, A.L.3
Randall, R.J.4
-
58
-
-
0033957834
-
The SWISS-PROT protein sequence database and its supplement TrEMBL in 2000
-
Bairoch, A.; Apweiler, R. The SWISS-PROT protein sequence database and its supplement TrEMBL in 2000 Nucleic Acids Res. 2000, 28, 45-48
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 45-48
-
-
Bairoch, A.1
Apweiler, R.2
-
59
-
-
36448991500
-
Clustal W and Clustal X version 2.0
-
Larkin, M. A.; Blackshields, G.; Brown, N. P.; Chenna, R.; McGettigan, P. A.; McWilliam, H.; Valentin, F.; Wallace, I. M.; Wilm, A.; Lopez, R.; Thompson, J. D.; Gibson, T. J.; Higgins, D. G. Clustal W and Clustal X version 2.0 Bioinformatics 2007, 23, 2947-2948
-
(2007)
Bioinformatics
, vol.23
, pp. 2947-2948
-
-
Larkin, M.A.1
Blackshields, G.2
Brown, N.P.3
Chenna, R.4
McGettigan, P.A.5
McWilliam, H.6
Valentin, F.7
Wallace, I.M.8
Wilm, A.9
Lopez, R.10
Thompson, J.D.11
Gibson, T.J.12
Higgins, D.G.13
-
60
-
-
0002051540
-
BioEdit: A user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT
-
Hall, T. A. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT Nucleic Acids Symp. Ser. 1999, 41, 95-98
-
(1999)
Nucleic Acids Symp. Ser.
, vol.41
, pp. 95-98
-
-
Hall, T.A.1
-
61
-
-
0027136282
-
Comparative protein modelling by satisfaction of spatial restraints
-
Sali, A.; Blundell, T. L. Comparative protein modelling by satisfaction of spatial restraints J. Mol. Biol. 1993, 234, 779-815
-
(1993)
J. Mol. Biol.
, vol.234
, pp. 779-815
-
-
Sali, A.1
Blundell, T.L.2
-
62
-
-
70450206724
-
-
revision B.01; Gaussian, Inc. Wallingford, CT
-
Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Scalmani, G.; Barone, V.; Mennucci, B.; Petersson, G. A.; Nakatsuji, H.; Caricato, M.; Li, X.; Hratchian, H. P.; Izmaylov, A. F.; Bloino, J.; Zheng, G.; Sonnenberg, J. L.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Vreven, T.; Montgomery, J. A., Jr.; Peralta, J. E.; Ogliaro, F.; Bearpark, M.; Heyd, J. J.; Brothers, E.; Kudin, K. N.; Staroverov, V. N.; Kobayashi, R.; Normand, J.; Raghavachari, K.; Rendell, A.; Burant, J. C.; Iyengar, S. S.; Tomasi, J.; Cossi, M.; Rega, N.; Millam, J. M.; Klene, M.; Knox, J. E.; Cross, J. B.; Bakken, V.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Martin, R. L.; Morokuma, K.; Zakrzewski, V. G.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Dapprich, S.; Daniels, A. D.; Farkas; Foresman, J. B.; Ortiz, J. V.; Cioslowski, J.; Fox, D. J. Gaussian 09, revision B.01; Gaussian, Inc.: Wallingford, CT, 2009.
-
(2009)
Gaussian 09
-
-
Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Scalmani, G.7
Barone, V.8
Mennucci, B.9
Petersson, G.A.10
Nakatsuji, H.11
Caricato, M.12
Li, X.13
Hratchian, H.P.14
Izmaylov, A.F.15
Bloino, J.16
Zheng, G.17
Sonnenberg, J.L.18
Hada, M.19
Ehara, M.20
Toyota, K.21
Fukuda, R.22
Hasegawa, J.23
Ishida, M.24
Nakajima, T.25
Honda, Y.26
Kitao, O.27
Nakai, H.28
Vreven, T.29
Montgomery Jr., J.A.30
Peralta, J.E.31
Ogliaro, F.32
Bearpark, M.33
Heyd, J.J.34
Brothers, E.35
Kudin, K.N.36
Staroverov, V.N.37
Kobayashi, R.38
Normand, J.39
Raghavachari, K.40
Rendell, A.41
Burant, J.C.42
Iyengar, S.S.43
Tomasi, J.44
Cossi, M.45
Rega, N.46
Millam, J.M.47
Klene, M.48
Knox, J.E.49
Cross, J.B.50
Bakken, V.51
Adamo, C.52
Jaramillo, J.53
Gomperts, R.54
Stratmann, R.E.55
Yazyev, O.56
Austin, A.J.57
Cammi, R.58
Pomelli, C.59
Ochterski, J.W.60
Martin, R.L.61
Morokuma, K.62
Zakrzewski, V.G.63
Voth, G.A.64
Salvador, P.65
Dannenberg, J.J.66
Dapprich, S.67
Daniels, A.D.68
Farkas69
Foresman, J.B.70
Ortiz, J.V.71
Cioslowski, J.72
Fox, D.J.73
more..
-
63
-
-
76149120388
-
AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading
-
Trott, O.; Olson, A. J. AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading J. Comput. Chem. 2010, 31, 455-461
-
(2010)
J. Comput. Chem.
, vol.31
, pp. 455-461
-
-
Trott, O.1
Olson, A.J.2
-
64
-
-
58049201323
-
-
University of California at San Francisco: San Francisco, CA
-
Case, D. A.; Darden, T. A.; Cheatham, T. E., III; Simmerling, C.L.; Wang, J.; Duke, R. E.; Luo, R.; Crowley, M.; Walker, R.C.; Zhang, W.; Merz, K. M.; Wang, B.; Hayik, S.; Roitberg, A.; Seabra, G.; Kolossváry, I.; Wong, K. F.; Paesani, F.; Vanicek, J.; Wu, X.; Brozell, S. R.; Steinbrecher, T.; Gohlke, H.; Yang, L.; Tan, C.; Mongan, J.; Hornak, V.; Cui, G.; Mathews, D. H.; Seetin, M. G.; Sagui, C.; Babin, V.; Kollman, P. A. AMBER 10; University of California at San Francisco: San Francisco, CA, 2008.
-
(2008)
AMBER 10
-
-
Case, D.A.1
Darden, T.A.2
Iii, E.C.T.3
Simmerling, C.L.4
Wang, J.5
Duke, R.E.6
Luo, R.7
Crowley, M.8
Walker, R.C.9
Zhang, W.10
Merz, K.M.11
Wang, B.12
Hayik, S.13
Roitberg, A.14
Seabra, G.15
Kolossváry, I.16
Wong, K.F.17
Paesani, F.18
Vanicek, J.19
Wu, X.20
Brozell, S.R.21
Steinbrecher, T.22
Gohlke, H.23
Yang, L.24
Tan, C.25
Mongan, J.26
Hornak, V.27
Cui, G.28
Mathews, D.H.29
Seetin, M.G.30
Sagui, C.31
Babin, V.32
Kollman, P.A.33
more..
-
65
-
-
33748518255
-
Comparison of multiple Amber force fields and development of improved protein backbone parameters
-
Hornak, V.; Abel, R.; Okur, A.; Strockbine, B.; Roitberg, A.; Simmerling, C. Comparison of multiple Amber force fields and development of improved protein backbone parameters Proteins 2006, 65, 712-725
-
(2006)
Proteins
, vol.65
, pp. 712-725
-
-
Hornak, V.1
Abel, R.2
Okur, A.3
Strockbine, B.4
Roitberg, A.5
Simmerling, C.6
-
66
-
-
2942532422
-
Development and testing of a general amber force field
-
Wang, J.; Wolf, R. M.; Caldwell, J. W.; Kollman, P. A.; Case, D. A. Development and testing of a general amber force field J. Comput. Chem. 2004, 25, 1157-1174
-
(2004)
J. Comput. Chem.
, vol.25
, pp. 1157-1174
-
-
Wang, J.1
Wolf, R.M.2
Caldwell, J.W.3
Kollman, P.A.4
Case, D.A.5
-
67
-
-
3042524904
-
A well-behaved electrostatic potential based method using charge restraints for deriving atomic charges: The RESP model
-
Bayly, C. I.; Cieplak, P.; Cornell, W.; Kollman, P. A. A well-behaved electrostatic potential based method using charge restraints for deriving atomic charges: the RESP model J. Phys. Chem. 1993, 97, 10269-10280
-
(1993)
J. Phys. Chem.
, vol.97
, pp. 10269
-
-
Bayly, C.I.1
Cieplak, P.2
Cornell, W.3
Kollman, P.A.4
|